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Frontiers | Basement Membrane Defects in Genetic Kidney Diseases
Figure 1 from Alport's syndrome, Goodpasture's syndrome, and type IV collagen. | Semantic Scholar
Collagen IVα345 dysfunction in glomerular basement membrane diseases. I. Discovery of a COL4A3 variant in familial Goodpasture's and Alport diseases - Journal of Biological Chemistry
Collagen IV Archives - Diapharma
Alport's Syndrome, Goodpasture's Syndrome, and Type IV Collagen | NEJM
Alport's Syndrome, Goodpasture's Syndrome, and Type IV Collagen | NEJM
Figure 2 from Type IV Collagens and Basement Membrane Diseases: Cell Biology and Pathogenic Mechanisms. | Semantic Scholar
Gly897Glu substitution in the type IV collagen 4 chain in BFH. Sequence... | Download Scientific Diagram
Alport's Syndrome, Goodpasture's Syndrome, and Type IV Collagen | NEJM
Alport Syndrome - Type IV collagen defect - Creative Med Doses
Type IV Collagen - an overview | ScienceDirect Topics
Frontiers | Basement Membrane Defects in Genetic Kidney Diseases
Schematic representation of type IV collagen biosynthesis and potential... | Download Scientific Diagram
IJMS | Free Full-Text | From Structure to Phenotype: Impact of Collagen Alterations on Human Health | HTML
Collagen Types and Linked Disorders
Immunostaining of different α(IV) collagen chains in Alport mouse... | Download Scientific Diagram
A Novel Heterozygous Mutation of the COL4A3 Gene Causes a Peculiar Phenotype without Hematuria and Renal Function Impairment in a Chinese Family
Type IV collagen: A network for development, differentiation, and disease - ScienceDirect
Type IV collagen: A network for development, differentiation, and disease - ScienceDirect
Mutations in Type IV Collagen and Their Clinical Significance in Kidney Disease - Renal Fellow Network
Collagen biology and non‐invasive biomarkers of liver fibrosis - Karsdal - 2020 - Liver International - Wiley Online Library
Collagen Type 4 - an overview | ScienceDirect Topics
Alport's Syndrome, Goodpasture's Syndrome, and Type IV Collagen | NEJM
Revision about hearing loss in the Alport's syndrome, analyzing the clinical, genetic and bio-molecular aspects - ScienceDirect